SERPINF2 Chromosome 17

Serpin family F member 2
9 variants 9 Health Risk

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What This Gene Does
This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Info
Gene Group
Serpin peptidase inhibitors
Locus Type
gene with protein product
Location
17p13.3
Ensembl
ENSG00000167711
Associated Conditions (2)
Alpha-2-plasmin inhibitor deficiency
Abnormal bleeding
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS142502473 Health Risk Conflicting classifications of pathogenicity —
RS144824741 Health Risk Conflicting classifications of pathogenicity —
RS144890920 Health Risk Conflicting classifications of pathogenicity —
RS201542762 Health Risk Conflicting classifications of pathogenicity —
RS200885603 Health Risk Likely pathogenic —
RS121965061 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
RS121965062 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
RS1597325785 Health Risk Pathogenic Abnormal bleeding, Abnormal bleeding
RS2543443583 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
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